Canonical Allele Identifier: CA2616085470

Gene: APOA5

Linked Data

• gnomAD v4: 11-116789988-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116789988C>A , CM000673.2:g.116789988C>A	GRCh38
NC_000011.9:g.116660704C>A , CM000673.1:g.116660704C>A	GRCh37
NC_000011.8:g.116165914C>A	NCBI36
NG_015894.1:g.7433G>T
NG_015894.2:g.7433G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000227665.9:c.*140G>T MANE Select	ENSP00000227665.4:n.*140G>T
ENST00000433069.2:c.*140G>T	ENSP00000399701.2:n.*140G>T
ENST00000227665.8:c.*140G>T	ENSP00000227665.4:n.*140G>T
ENST00000542499.5:c.*140G>T	ENSP00000445002.1:n.*140G>T
NM_001166598.1:c.*140G>T	NP_001160070.1:n.*140G>T
NM_052968.4:c.*140G>T	NP_443200.2:n.*140G>T
NM_001166598.2:c.*140G>T	NP_001160070.1:n.*140G>T
NM_001371904.1:c.*140G>T MANE Select	NP_001358833.1:n.*140G>T
NM_052968.5:c.*140G>T	NP_443200.2:n.*140G>T